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Summary Literature (0)
DOID:0060241 - 3-M syndrome


Disease Ontology Definition:A syndrome characterized by dwarfism, facial dysmorphia and skeletal abnormalities.

Synonyms: Le Merrer syndrome, Miller-McKusick-Malvaux syndrome, Yakut short stature syndrome, dolichospondylic dysplasia, gloomy face syndrome, three M syndrome

In OMIM:
OMIM:273750 - THREE M SYNDROME 1; 3M1
OMIM:612921 - THREE M SYNDROME 2; 3M2
OMIM:614205 - THREE M SYNDROME 3; 3M3

In Mondo Disease Ontology:
MONDO:0007477 - 3-M syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : obsl1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)